A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3237n54



Internal ID22771132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:70157106..70204085hg38UCSC Ensembl
chr13:70731238..70778217hg19UCSC Ensembl
chr13:69629239..69676218hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3846980
hg1946980
hg1846980
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv562239, nsv562227, nsv562233, nsv562229, nsv562225, nsv562240, nsv562238, nsv562226, nsv562228, nsv562224, nsv562232, nsv562235, nsv562234
Samples1780862384_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3237n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss48
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer